Integrating adipocyte insulin signaling and metabolism in the multi-omics era.

Trends Biochem Sci

Program in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA. Electronic address:

Published: June 2022

Insulin stimulates glucose uptake into adipocytes via mTORC2/AKT signaling and GLUT4 translocation and directs glucose carbons into glycolysis, glycerol for TAG synthesis, and de novo lipogenesis. Adipocyte insulin resistance is an early indicator of type 2 diabetes in obesity, a worldwide health crisis. Thus, understanding the interplay between insulin signaling and central carbon metabolism pathways that maintains adipocyte function, blood glucose levels, and metabolic homeostasis is critical. While classically viewed through the lens of individual enzyme-substrate interactions, advances in mass spectrometry are beginning to illuminate adipocyte signaling and metabolic networks on an unprecedented scale, yet this is just the tip of the iceberg. Here, we review how 'omics approaches help to elucidate adipocyte insulin action in cellular time and space.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109456PMC
http://dx.doi.org/10.1016/j.tibs.2022.02.009DOI Listing

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